New Life Corporation
FDA import alert and refusal historyDavid, PanamaFEI 3004674891
As of October 26, 2026, New Life Corporation (David, Panama) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for anchovy; blue fish; all histamine producing fish species, published by FDA on August 29, 2012, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for New Life Corporation
2 records, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 16-120red listAnchovy; Blue Fish; All histamine producing fish speciesSource
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about New Life Corporation
- Is New Life Corporation on an FDA import alert?
- Yes. As of October 26, 2026, New Life Corporation is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for anchovy; blue fish; all histamine producing fish species; FDA published the listing on August 29, 2012.
- Has FDA refused shipments from New Life Corporation?
- No FDA import refusals for New Life Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was New Life Corporation last inspected by FDA?
- FDA's most recent inspection of New Life Corporation with a final classification is dated July 19, 2011 and was classified VAI (Voluntary Action Indicated).
- What is New Life Corporation's FEI number?
- New Life Corporation's FDA Establishment Identifier (FEI) is 3004674891.
- Can shipments from New Life Corporation still enter the U.S.?
- Shipments of anchovy; blue fish; all histamine producing fish species from New Life Corporation can be detained without physical examination under Import Alert 16-120; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.